Similar Jobs
See allClinical Coordinator
Tiny Health
North America
Clinical Research
Regulatory Compliance
Project Management
Trial Documentation Associate I
St. Jude Children’s Research Hospital
US
Clinical Research
Document Management
Regulatory Compliance
FSP Vendor Management Specialist
Not Disclosed
Brazil
Clinical Operations
Vendor Management
Project Management
Senior Clinical Research Associate
Undisclosed
US
Clinical Monitoring
Regulatory Knowledge
Site Management
Global Clinical Supplies Operational Bidding Specialist
Partner Company
Brazil
Budgeting
Proposal Management
Microsoft Excel
Role Overview:
- Support clinical trial activities across multiple functional areas including patient engagement, study operations, and regulatory affairs.
- Coordinate participant visits, recruitment, and screening with strong attention to regulatory compliance and documentation.
- Communicate effectively with sponsors, CROs, and study sites to ensure seamless study progression.
Requirements:
- 2-3 years of relevant clinical trial support experience in research sites, CROs, or sponsor organizations.
- Strong knowledge of GCP, ICH E6(R3), and HIPAA, with experience in CTMS, EDC, or eRegulatory systems.
- Excellent organizational, documentation, and independent working skills in a remote environment.
Benefits & Culture:
- Fully remote work with flexible full-time, part-time, or project-based opportunities.
- Exposure to diverse therapeutic areas and clinical trial lifecycle stages for professional growth.
- Contribution to ethical, scientifically rigorous research supporting new treatment development.
Jobgether
This partner company supports fast-growing remote clinical research environments, helping keep clinical trials organized, compliant, and moving forward. They collaborate with research sites, sponsors, CROs, and healthcare organizations globally, offering multidisciplinary roles in a remote setting.